Canonical Allele Identifier: CA2657584093

Gene: CHKB CHKB-CPT1B

Linked Data

• gnomAD v4: 22-50582094-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50582094C>T , CM000684.2:g.50582094C>T	GRCh38
NC_000022.10:g.51020523C>T , CM000684.1:g.51020523C>T	GRCh37
NC_000022.9:g.49367389C>T	NCBI36
NG_012643.1:g.1574G>A
NG_029213.1:g.5906G>A , LRG_855:g.5906G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406938.3:c.333+155G>A (CHKB) MANE Select	ENSP00000384400.3:n.333+155G>A
ENST00000406938.2:c.333+155G>A (CHKB)	ENSP00000384400.2:n.333+155G>A
ENST00000463053.1:n.417G>A (CHKB)
ENST00000465842.1:n.172+155G>A (CHKB)
ENST00000468532.5:n.210+155G>A (CHKB)
ENST00000476289.5:n.606+155G>A (CHKB)
ENST00000479003.5:n.727G>A (CHKB)
ENST00000481673.5:n.552G>A (CHKB)
ENST00000484266.5:n.576+155G>A (CHKB)
ENST00000492556.5:n.872G>A (CHKB-CPT1B)
ENST00000492582.5:n.761G>A (CHKB)
NM_005198.4:c.333+155G>A , LRG_855t1:c.333+155G>A (CHKB)	NP_005189.2:n.333+155G>A
NR_027928.2:n.551+155G>A (CHKB-CPT1B)
NM_005198.5:c.333+155G>A (CHKB) MANE Select	NP_005189.2:n.333+155G>A